Author:
van der Linde I. H. M.,Hiemstra Y. L.,Bökenkamp R.,van Mil A. M.,Breuning M. H.,Ruivenkamp C.,ten Broeke S. W.,Veldkamp R. F.,van Waning J. I.,van Slegtenhorst M. A.,van Spaendonck-Zwarts K. Y.,Lekanne Deprez R. H.,Herkert J. C.,Boven L.,van der Zwaag P. A.,Jongbloed J. D. H.,Bootsma M.,Barge-Schaapveld D. Q. C. M.
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Reference30 articles.
1. Gomez J, Reguero JR, Moris C, et al. Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor next-generation sequencing. Clin J. 2014;78:2963–71.
2. Kayvanpour E, Sedaghat-Hamedani F, Amr A, et al. Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals. Clin Res Cardiol. 2017;106:127–39.
3. Morales A, Painter T, Li R, et al. Rare variant mutations in pregnancy-associated or peripartum cardiomyopathy. Circulation. 2010;121:2176–82.
4. Hoedemaekers YM, Caliskan K, Michels M, et al. The importance of genetic counseling, DNA diagnostics, and cardiologic family screening in left ventricular noncompaction cardiomyopathy. Circ Cardiovasc Genet. 2010;3:232–9.
5. Fiorillo C, Astrea G, Savarese M, et al. MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients. Orphanet J Rare Dis. 2016;11:91.
Cited by
18 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献